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Herein, we report on a two-dimensional amino-functionalized Ti3C2-MXene (N–Ti3C2-MXene)-based surface plasmon resonance (SPR) biosensor for detecting carcinoembryonic antigen (CEA) utilizing a sandwich format signal amplification strategy. Our biosensor employs an N-Ti3C2-MXene nanosheet-modified sensing platform and a signal enhancer comprising N-Ti3C2-MXene-hollow gold nanoparticles (HGNPs)-staphylococcal protein A (SPA) complexes. Ultrathin Ti3C2-MXene nanosheets were synthesized and functionalized with aminosilane to provide a hydrophilic-biocompatible nanoplatform for covalent immobilization of the monoclonal anti-CEA capture antibody (Ab1). The N-Ti3C2-MXene/HGNPs nanohybrids were synthesized and further decorated with SPA to immobilize the polyclonal anti-CEA detection antibody (Ab2) and serve as signal enhancers. The capture of CEA followed by the formation of the Ab2-conjugated SPA/HGNPs/N-Ti3C2-MXene sandwiched nanocomplex on the SPR chip results in the generation of a response signal. The fabricated N-Ti3C2-MXene-based SPR biosensor exhibited a linear detection range of 0.001–1000 PM with a detection limit of 0.15 fM. The proposed biosensor showed high sensitivity and specificity for CEA in serum samples, which gives it application potential in the early diagnosis and monitoring of cancer. We believe that this work also opens new avenues for development of MXene-based highly sensitive biosensors for determining various biomolecules.

Metallic phase molybdenum disulfide (1T-MoS 2 ), with its fast carrier mobility and highly abundant active sites, plays a vital role in the field of catalysis. However, the development of a simple and efficient strategy for the preparation of stabilized 1T-MoS 2 remains a great challenge. Herein, we report the spontaneous phase transformation of MoS 2 from the 2H to the 1T phase, caused by the strong metal−support interaction during iridium (Ir) adsorption. The resulting Ir/MoS 2 heterostructures show higher catalytic activity for overall water splitting than those of commercial Pt/C and IrO 2 in alkaline media. We believe that the spontaneous phase transformation of this material not only opens up a new perspective for developing advanced catalysts for alkaline water splitting but also presents an efficient and intriguing method for the phase engineering of two-dimensional materials.

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